English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Hunting the eagle killer: A cyanobacterial neurotoxin causes vacuolar myelinopathy

MPS-Authors
/persons/resource/persons210396

Geier,  Benedikt
Department of Symbiosis, Max Planck Institute for Marine Microbiology, Max Planck Society;

/persons/resource/persons210577

Liebeke,  Manuel
Department of Symbiosis, Max Planck Institute for Marine Microbiology, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

science.aax9050.pdf
(Publisher version), 2MB

Supplementary Material (public)
There is no public supplementary material available
Citation

Breinlinger, S., Phillips, T. J., Haram, B. N., Mares, J., Yerena, J. A. M., Hrouzek, P., et al. (2021). Hunting the eagle killer: A cyanobacterial neurotoxin causes vacuolar myelinopathy. SCIENCE, 371(6536), 1335-+. doi:10.1126/science.aax9050.


Cite as: https://hdl.handle.net/21.11116/0000-0009-823E-F
Abstract
Vacuolar myelinopathy is a fatal neurological disease that was initially discovered during a mysterious mass mortality of bald eagles in Arkansas in the United States. The cause of this wildlife disease has eluded scientists for decades while its occurrence has continued to spread throughout freshwater reservoirs in the southeastern United States. Recent studies have demonstrated that vacuolar myelinopathy is induced by consumption of the epiphytic cyanobacterial species Aetokthonos hydrillicola growing on aquatic vegetation, primarily the invasive Hydrilla verticillata. Here, we describe the identification, biosynthetic gene cluster, and biological activity of aetokthonotoxin, a pentabrominated biindole alkaloid that is produced by the cyanobacterium A. hydrillicola. We identify this cyanobacterial neurotoxin as the causal agent of vacuolar myelinopathy and discuss environmental factors-especially bromide availability-that promote toxin production.